HGVS | Genome Assembly |
---|---|
NC_000012.12:g.66211343A>C , CM000674.2:g.66211343A>C | GRCh38 |
NC_000012.11:g.66605123A>C , CM000674.1:g.66605123A>C | GRCh37 |
NC_000012.10:g.64891390A>C | NCBI36 |
NG_021194.1:g.27146A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261233.9:c.437-103A>C MANE Select | ENSP00000261233.4:n.437-103A>C | |
ENST00000261233.8:c.437-103A>C | ENSP00000261233.4:n.437-103A>C | |
ENST00000457197.2:c.254-103A>C | ENSP00000409852.2:n.254-103A>C | |
NM_001142523.1:c.254-103A>C | NP_001135995.1:n.254-103A>C | |
NM_007199.2:c.437-103A>C | NP_009130.2:n.437-103A>C | |
NM_001142523.2:c.254-103A>C | NP_001135995.1:n.254-103A>C | |
NM_007199.3:c.437-103A>C MANE Select | NP_009130.2:n.437-103A>C |